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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 1
1995 4
1996 2
1998 1
2001 3
2002 4
2003 3
2004 4
2005 2
2006 1
2007 1
2008 4
2009 3
2010 6
2011 5
2012 5
2013 2
2014 7
2015 5
2016 4
2017 6
2018 3
2019 5
2020 5
2021 2
2022 2
2023 1
2024 0

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83 results

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Page 1
Clinical variability in ataxia-telangiectasia.
Lohmann E, Krüger S, Hauser AK, Hanagasi H, Guven G, Erginel-Unaltuna N, Biskup S, Gasser T. Lohmann E, et al. Among authors: erginel unaltuna n. J Neurol. 2015 Jul;262(7):1724-7. doi: 10.1007/s00415-015-7762-z. Epub 2015 May 10. J Neurol. 2015. PMID: 25957637
[A new indicator in coronary artery diseases].
Erginel Ünaltuna N. Erginel Ünaltuna N. Turk Kardiyol Dern Ars. 2020 Sep;48(6):555-557. doi: 10.5543/tkda.2020.65977. Turk Kardiyol Dern Ars. 2020. PMID: 32955032 Free article. Turkish. No abstract available.
Mutations in TYROBP are not a common cause of dementia in a Turkish cohort.
Darwent L, Carmona S, Lohmann E, Guven G, Kun-Rodrigues C, Bilgic B, Hanagasi H, Gurvit H, Erginel-Unaltuna N, Pak M, Hardy J, Singleton A, Brás J, Guerreiro R. Darwent L, et al. Among authors: erginel unaltuna n. Neurobiol Aging. 2017 Oct;58:240.e1-240.e3. doi: 10.1016/j.neurobiolaging.2017.06.019. Epub 2017 Jun 28. Neurobiol Aging. 2017. PMID: 28716534 Free PMC article.
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.
Atasu B, Hanagasi H, Bilgic B, Pak M, Erginel-Unaltuna N, Hauser AK, Guven G, Simón-Sánchez J, Heutink P, Gasser T, Lohmann E. Atasu B, et al. Among authors: erginel unaltuna n. Mov Disord. 2018 Aug;33(8):1354-1358. doi: 10.1002/mds.27442. Epub 2018 Aug 25. Mov Disord. 2018. PMID: 30145809
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.
Kessler C, Atasu B, Hanagasi H, Simón-Sánchez J, Hauser AK, Pak M, Bilgic B, Erginel-Unaltuna N, Gurvit H, Gasser T, Lohmann E. Kessler C, et al. Among authors: erginel unaltuna n. Parkinsonism Relat Disord. 2018 Mar;48:34-39. doi: 10.1016/j.parkreldis.2017.12.007. Epub 2017 Dec 9. Parkinsonism Relat Disord. 2018. PMID: 29248340
83 results